eudamed_udi
Primary ID: 08426950013204
RF plus Calibrator (UDI 08426950013204)
Manufactured by Biokit S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RF plus Calibrator - Primary ID 08426950013204
Device Regulatory Overview
The RF plus Calibrator (Model/Catalog Number: 3000-2252) is a medical device manufactured by Biokit S.A.. This product is indexed under FDA Product Code / Category Classification W01021110 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3000-2252
- Product Code / EMDN
- W01021110
- Device Name
- RF (II)
- Database Sync Date
- 2026-08-09 16:48:38
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of RF plus Calibrator?
The registered manufacturer of record for RF plus Calibrator is Biokit S.A..
What is the Primary UDI-DI identifier for RF plus Calibrator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08426950013204.
What classification code is assigned to this device?
This device is registered under product classification code W01021110.
Similar Classification Devices (W01021110)
Other Devices by Biokit S.A.
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